Source:http://linkedlifedata.com/resource/pubmed/id/21412816
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
2011-4-14
|
pubmed:abstractText |
Although mononuclear cells (MNCs) from bone marrow are being investigated in phase I clinical trials in stroke patients, dose response, therapeutic time window, and biodistribiton have not been well-characterized in animal stroke models. Long Evans rats underwent common carotid artery/middle cerebral artery occlusion (CCA/MCAo) and 24 hr later were randomized to receive saline IV or a bone marrow aspiration followed by an IV infusion of autologous separated MNCs (1 million, 10 million, or 30 million cells/kg). In another experiment, rats underwent CCAo/MCAo and were randomized at 24 hr, 72 hr, or 7 days after stroke to receive a saline injection or 10 million/kg MNCs. All animals were evaluated on the cylinder and corner tests up to 28 days. MNCs were tracked using Q-dot nanocrystals to monitor biodistribution. Animals treated with MNCs at 10 million and 30 million cells/kg at 24 hr after stroke had significant reductions in neurological deficits and lesion size compared with saline controls or animals treated with 1 million cells/kg. There was no difference in neurological deficits in the 10 and 30 million cell/kg groups at 28 days. Animals treated with MNCs at 72 hr but not at 7 days showed a significant reduction in neurological deficits by 28 days. Labeled MNCs were found in the brain, spleen, lung, liver, and kidney at 1 hr and exponentially decreased over the ensuing week. In conclusion, we found a maximum reduction in neurological deficits at 10 and 30 million cells/kg and a therapeutic time window up to 72 hr after stroke. © 2011 Wiley-Liss, Inc.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
1097-4547
|
pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2011 Wiley-Liss, Inc.
|
pubmed:issnType |
Electronic
|
pubmed:volume |
89
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
833-9
|
pubmed:meshHeading |
pubmed-meshheading:21412816-Analysis of Variance,
pubmed-meshheading:21412816-Animals,
pubmed-meshheading:21412816-Bone Marrow Cells,
pubmed-meshheading:21412816-Bone Marrow Transplantation,
pubmed-meshheading:21412816-Brain Infarction,
pubmed-meshheading:21412816-Disease Models, Animal,
pubmed-meshheading:21412816-Infarction, Middle Cerebral Artery,
pubmed-meshheading:21412816-Injections, Intravenous,
pubmed-meshheading:21412816-Male,
pubmed-meshheading:21412816-Movement Disorders,
pubmed-meshheading:21412816-Rats,
pubmed-meshheading:21412816-Rats, Long-Evans,
pubmed-meshheading:21412816-Time Factors,
pubmed-meshheading:21412816-Transplantation, Autologous
|
pubmed:year |
2011
|
pubmed:articleTitle |
Therapeutic time window and dose response of autologous bone marrow mononuclear cells for ischemic stroke.
|
pubmed:affiliation |
Department of Neurology, University of Texas Medical School at Houston, Houston, TX 77030, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
|